| Literature DB >> 30711802 |
Giovanna Piovani1, Gaetana Lanzi2, Rosalba Monica Ferraro2, Stefania Masneri2, Chiara Barisani2, Giulia Savio3, Silvia Clara Giliani2.
Abstract
The Cri du Chat Syndrome (CdCS) is a genetic disease resulting from variable size deletion occurring on the short arm of chromosome 5. The main clinical features are a high-pitched monochromatic cry, microcephaly, severe psychomotor and mental retardation with characteristics of autism spectrum disorders such as hand flapping, obsessive attachments to objects, twirling objects, repetitive movements, and rocking. We reprogrammed to pluripotency peripheral blood mononuclear cells derived from a patient carrying large deletion on the short arm of chromosome 5, using a commercially available non-integrating expression system. The iPSCs expressed pluripotency markers and differentiated in the three embryonic germ layers.Entities:
Mesh:
Year: 2019 PMID: 30711802 DOI: 10.1016/j.scr.2019.101393
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020